NCT02905357Active, not recruiting
Heart Attack Research Program- Imaging Study
Source: ClinicalTrials.gov · Last updated 19 Mar 2026
Brief summary (registry, in English)
The HARP study is a multi-center, diagnostic observational study employing standardized imaging protocols in patients with MINOCA (MI with Non Obstructive Coronary Arteries) to determine the underlying diagnosis in each participant. Participants will be followed for recurrent clinical events, every 6 months, for a maximum of 10 years.
- Status (registry)
- Active, not recruiting
- Study type
- Observational
- Enrollment
- 450 (estimated)
- First submitted
- 9 Sept 2016
- Start date
- 12 Sept 2016
- Primary completion date
- 30 Jun 2027
- Lead sponsor
- NYU Langone Health
- Diseases
- Coronary artery disease
- NCT number
- NCT02905357
What you commit to
- Study type: Observational
- Planned participants: 450
- From 12 Sept 2016 to the primary completion date, 30 Jun 2027
- 20 sites in 3 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Contraindication to MRI (including but not limited to ferromagnetic implants)
- Thrombolytic therapy for STEMI (qualifying event)
Other illness
- Stenosis ≥50% of any major epicardial vessel on invasive angiography, as determined by the angiographer at the time of clinically ordered cardiac catheterization
- History of known obstructive coronary artery disease at angiography, including history of percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG)
- Alternate explanation for troponin elevation, such as hypertensive urgency, acute exacerbation of heart failure, chronic elevation due to kidney disease, pulmonary embolism, cardiac trauma
Lab values
- eGFR\<45 or contraindication to additional contrast needed for OCT in the opinion of the angiographer or treating physician
Other
- Recent use of vasospastic agents, such as cocaine, triptans, or ergot alkaloids (≤1 month)
- Coronary dissection apparent on angiography
- Excessive coronary tortuosity which, in the angiographer's opinion, increases the risks of OCT
- Pregnancy
Who the study is looking for
- Acute ischemic symptoms compatible with diagnosis of MI, such as chest pain or anginal equivalent symptoms at rest or new onset exertional anginal equivalent symptoms
- Objective evidence of MI (either or both of the following):
- Elevation of troponin to above the laboratory upper limit of normal
- ST segment elevation of ≥1mm on 2 contiguous ECG leads
- Willing to provide informed consent and comply with all aspects of the protocol
- Age ≥ 21 years
Age in the registry: 21 years to 99 years · Sex: All · Does not accept healthy volunteers
Sites (20)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University Of Calgary Coordinator of this site? Confirm its status | Calgary | Canada | Unknown status |
| University of Alberta Coordinator of this site? Confirm its status | Edmonton | Canada | Unknown status |
| Vancouver General Hospital Coordinator of this site? Confirm its status | Vancouver | Canada | Unknown status |
| St. Boniface General Hospital Coordinator of this site? Confirm its status | Winnipeg | Canada | Unknown status |
| Golden Jubilee National Hospital Coordinator of this site? Confirm its status | Clydebank | United Kingdom | Unknown status |
| Emory University Coordinator of this site? Confirm its status | Atlanta | United States | Unknown status |
| Seton Heart (Ascension) Univeristy of Austin, Texas Coordinator of this site? Confirm its status | Austin | United States | Unknown status |
| Johns Hopkins Medical Center Coordinator of this site? Confirm its status | Baltimore | United States | Unknown status |
| St. Luke's University Health Network Coordinator of this site? Confirm its status | Bethlehem | United States | Unknown status |
| University of Alabama Birmingham Coordinator of this site? Confirm its status | Birmingham | United States | Unknown status |
| Ohio State University Medical Center Coordinator of this site? Confirm its status | Columbus | United States | Unknown status |
| University of Florida Medical Center Coordinator of this site? Confirm its status | Gainesville | United States | Unknown status |
| Dartmouth Hitchcock Coordinator of this site? Confirm its status | Lebanon | United States | Unknown status |
| Cedars-Sinai Medical Center Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
| NYU Winthrop Coordinator of this site? Confirm its status | Mineola | United States | Unknown status |
| NYU Langone Medical Center Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| Columbia University Medical Center/NYPH Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| University of Pittsburgh Medical Center Coordinator of this site? Confirm its status | Pittsburgh | United States | Unknown status |
| UC San Diego Medical Center Coordinator of this site? Confirm its status | San Diego | United States | Unknown status |
| Stanford University Coordinator of this site? Confirm its status | Stanford | United States | Unknown status |
Related publications
- Accuracy of Angiographic Identification of Culprit Lesions in Women With MINOCA.Circ Cardiovasc Interv · 2026 · PMID 42717865
This page is information, not medical advice. Discuss any trial with your doctor.